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2015年先天性胆管扩张症诊断标准

Diagnostic criteria for congenital biliary dilatation 2015.

作者信息

Hamada Yoshinori, Ando Hisami, Kamisawa Terumi, Itoi Takao, Urushihara Naoto, Koshinaga Tsugumichi, Saito Takeshi, Fujii Hideki, Morotomi Yoshiki

机构信息

Division of Pediatric Surgery, Department of Surgery, Kansai Medical University, Hirakata City, Osaka, Japan.

Aichi Prefectural Colony, Kasugai, Japan.

出版信息

J Hepatobiliary Pancreat Sci. 2016 Jun;23(6):342-6. doi: 10.1002/jhbp.346. Epub 2016 May 3.

Abstract

BACKGROUND

The Diagnostic Criteria for Pancreaticobiliary Maljunction 2013 were published by the Japanese Study Group on Pancreaticobiliary Maljunction (JSGPM) in 2014. The committee of JSGPM for diagnostic criteria for pancreaticobiliary maljunction has established the standard diameter of the bile duct, and a definition of dilatation of the bile duct was proposed in 2014.

METHODS

The committee of JSGPM prepared the diagnostic criteria for congenital biliary dilatation in 2014, and a final revised version was approved in 2015.

RESULTS

Congenital biliary dilatation is defined as a congenital malformation involving both local dilatation of the extrahepatic bile duct, including the common bile duct, and pancreaticobiliary maljunction. However, cases associated with intrahepatic bile duct dilatation can also be included. Various kinds of pathological conditions can occur on hepatobiliary systems and pancreas by bile duct dilatation and pancreaticobiliary maljunction. For a diagnosis of congenital biliary dilatation, both abnormal dilatation of the bile duct and pancreaticobiliary maljunction must be evident by either imaging test or anatomical examination. Acquired or secondary dilatation of the bile duct by obstruction due to biliary stones or malignancy should be strictly excluded.

CONCLUSION

Diagnostic criteria for congenital biliary dilatation 2015 were established from Japan representing a world first.

摘要

背景

日本胆胰管连接异常研究组(JSGPM)于2014年发布了《2013年胆胰管连接异常诊断标准》。JSGPM胆胰管连接异常诊断标准委员会确定了胆管的标准直径,并于2014年提出了胆管扩张的定义。

方法

JSGPM委员会于2014年制定了先天性胆管扩张的诊断标准,并于2015年批准了最终修订版。

结果

先天性胆管扩张被定义为一种先天性畸形,包括肝外胆管(包括胆总管)的局部扩张以及胆胰管连接异常。然而,伴有肝内胆管扩张的病例也可包括在内。胆管扩张和胆胰管连接异常可导致肝胆系统和胰腺出现各种病理状况。对于先天性胆管扩张的诊断,胆管异常扩张和胆胰管连接异常必须通过影像学检查或解剖检查明确显示。必须严格排除由胆结石或恶性肿瘤阻塞导致的后天性或继发性胆管扩张。

结论

2015年先天性胆管扩张诊断标准由日本制定,属世界首创。

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